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从手术标本制备的人肺微粒体组分对苯并(a)芘的氧化生物转化作用。

Oxidative biotransformation of benzo(a)pyrene by human lung microsomal fractions prepared from surgical specimens.

作者信息

Sípal Z, Ahlenius T, Bergstrand A, Rodriquez L, Jakobsson S W

出版信息

Xenobiotica. 1979 Oct;9(10):633-45. doi: 10.3109/00498257909042330.

DOI:10.3109/00498257909042330
PMID:532213
Abstract
  1. Microsomal fractions were prepared from 15--50 g specimens of human lung tissue (mostly alveolar) obtained at surgical resections of 13 middle-aged male patients suffering from different pulmonary tumours. Marker enzyme assays indicated that the frations contained about 25% of the endoplasmic reticulum of the homogenate and about 10% of its mitochondrial membranes. 2. The content of cytochrome b5 corresponded to that of rodent lung microsomes, whereas the apparent content of cytochrom P-450 was much lower. 3. The extent of benzo(a)pyrene metabolism varied 13-fold between individuals in the group and was not detectable in about 40% of the cases. 4. The dihydrodiols as % of total metabolites formed was higher than in laboratory animals, the 7,8-dihydrodiol in most cases amounting to more than 40% of total dihydrodiols. 5. The apparent rate of hydroxylation was stimulated by 1 mM 2-diethylaminothyl 2,2-diphenylvalerate and by 1 mM 1,2-oxy-3,3,3-trichloropropane, but inhibited moderately by 0.1 mM metyrapone and extensively by 0.05 mM 7,8-benzoflavone. 6. Ethoxyresorufin deethylation qualitatively paralleled benzo(a)pyrene hydroxylation among individuals.
摘要
  1. 从13名患有不同肺部肿瘤的中年男性患者手术切除获取的15 - 50克人肺组织标本(主要是肺泡组织)中制备微粒体部分。标记酶分析表明,这些部分含有匀浆中约25%的内质网和约10%的线粒体膜。2. 细胞色素b5的含量与啮齿动物肺微粒体的含量相当,而细胞色素P - 450的表观含量则低得多。3. 该组个体间苯并(a)芘代谢程度相差13倍,约40%的病例检测不到。4. 二氢二醇占总代谢产物的百分比高于实验动物,大多数情况下7,8 - 二氢二醇占总二氢二醇的40%以上。5. 1 mM 2 - 二乙氨基乙基2,2 - 二苯基戊酸酯和1 mM 1,2 - 氧 - 3,3,3 - 三氯丙烷刺激了表观羟化速率,但0.1 mM甲吡酮适度抑制,0.05 mM 7,8 - 苯并黄酮则广泛抑制。6. 个体中乙氧试卤灵脱乙基作用在质量上与苯并(a)芘羟化作用平行。

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Oxidative biotransformation of benzo(a)pyrene by human lung microsomal fractions prepared from surgical specimens.从手术标本制备的人肺微粒体组分对苯并(a)芘的氧化生物转化作用。
Xenobiotica. 1979 Oct;9(10):633-45. doi: 10.3109/00498257909042330.
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Carcinogenesis. 1981;2(9):919-26. doi: 10.1093/carcin/2.9.919.
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Species-specific enhancement by 7,8-benzoflavone of hepatic microsomal metabolism of benzo[e]pyrene 9,10-dihydrodiol to bay-region diol epoxides.7,8-苯并黄酮对苯并[e]芘9,10-二氢二醇向湾区二醇环氧化物的肝微粒体代谢的种属特异性增强作用。
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